A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955



Internal ID15552976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21603619..21648274hg38UCSC Ensembl
Outerchr13:22177758..22222413hg19UCSC Ensembl
Outerchr13:21075758..21120413hg18UCSC Ensembl
Outerchr13:21075758..21120413hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3844656
hg1944656
hg1844656
hg1744656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9093
SamplesNA12156
Known GenesMICU2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv955
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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